Medical Reviewer/Safety Reviewer III

Job Summary

Ready to leverage your expertise in medical review to shape promotional materials and drive strategic initiatives? We're seeking a Medical Reviewer/Safety Reviewer III to join our team on a contract basis. In this hybrid role based in Florham Park, NJ, you'll be instrumental in ensuring the accuracy and compliance of branded and unbranded content by providing crucial medical input throughout the Medical, Legal, and Regulatory (MLR) review process. You'll also take the lead on various projects, from medical education to digital communications, all while collaborating with a diverse group of cross-functional colleagues.

This is an excellent opportunity for someone with at least 3 years of experience in ad/promo medical review and a strong understanding of medical affairs. We're looking for a leader with an advanced scientific degree who can effectively manage multiple priorities and thrive in a dynamic, fast-paced environment. If you have a keen eye for detail, strong communication skills, and a passion for ensuring medical accuracy and regulatory compliance, we encourage you to apply.

location: Florham Park, New Jersey

job type: Contract

salary: $45.00 - 52.28 per hour

work hours: 9 to 5

education: Doctorate

Responsibilities

• Represent medical affairs in the Medical, Legal, and Regulatory (MLR) review process to ensure compliance with industry regulations and guidelines.
• Review promotional materials according to policies, guidelines, and customer needs.
• Support projects such as MSL activities, medical education initiatives, digital communications, and conference preparations and reports.
• Lead assigned projects, ensuring timely and excellent results.
• Collaborate with cross-functional colleagues to align and execute projects.
  
  

Qualifications

Required Skills and Qualifications:

• 3 years of experience in ad/promo medical review.
• 3 years of experience in the pharmaceutical industry or equivalent, with a strong understanding of medical affairs.
• Excellent collaborative and project management skills.
• Strong understanding of Medical, Legal, and Regulatory (MLR) processes.
• Effective oral and written communication skills, including the ability to present technical information.
• Strong analytical and problem-solving abilities.
• Attention to detail and strategic thinking.
• Strong leadership skills.
• Ability to thrive in a fast-paced environment and manage multiple priorities.
• Ability to adapt to changing business needs.
• Familiarity with interpreting scientific evidence and knowledge of the patient treatment journey.
  
  

Preferred Skills And Qualifications

• Company Medical Review experience (specifically with Veeva promo mat and med-com).
• An advanced scientific degree (PharmD, PhD, PA, or NP).
• Experience in CNS/Psychiatry.
• Experience with competitive reviews and publication analyses.
  
  

skills: Veeva Vault, Medical Science Liaison (MSL)

Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com.

Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility).

This posting is open for thirty (30) days.

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